A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180488



Internal ID20747528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80354904..80551922hg38UCSC Ensembl
chr16:80388801..80585819hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38197019
hg19197019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511919
Supporting Variants
Samples
Known GenesDYNLRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180488
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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